Haematopoietic stem/progenitor cells
AssigneeMurdoch Childrens Research Institute
InventorsElizabeth Ng, Edouard Stanley, Andrew Elefanty
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AssigneeMurdoch Childrens Research Institute
InventorsElizabeth Ng, Edouard Stanley, Andrew Elefanty
Estimating the term…
The invention relates to an isolated cell having, after culturing a pluripotent stem cell (PSC) in a medium comprising a WNT agonist and an ACTIVIN antagonist, increased HOXA gene expression relative to a PSC not cultured in a medium comprising a WNT agonist and an ACTIVIN antagonist, wherein the cell with increased HOXA gene expression is capable of generating a definitive haematopoietic stem/precursor cell. The invention also relates to use of the cell for generating a definitive haematopoietic stem/precursor cell, and a method for differentiating a PSC into a definitive haematopoietic stem/precursor cell and a definitive haematopoietic stem/progenitor cell differentiated from a PSC by the method. The invention further relates to a therapeutic composition comprising a cell of the invention, and to therapeutic methods and uses of a cell of the invention. The invention also relates to a reporter cell comprising distinguishable SOX17 and RUNXIC reporters, for use in tracking the differentiation of a PSC into a definitive haematopoietic stem/progenitor cell.
A method for differentiating a pluripotent stem cell (PSC) into a definitive haematopoietic stem/progenitor cell, the method comprising increasing HOXA gene expression by culturing the PSC as an embryoid body in a medium and adding a WNT agonist and an ACTIVIN antagonist to the medium at about day 2 to day 4, wherein the medium further comprises a retinoid or retinoic acid analogue added to the medium from day 2 or day 3, and wherein increased HOXA gene expression is relative to a cell net cultured in the medium to which the WNT agonist and the ACTIVIN antagonist are not added.
Dependencies are inferred from the claim text.